Variant #0000455666 (NC_000006.11:g.109787710G>A, NM_014797.2:c.1438C>T (ZBTB24))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.109787710G>A
DNA change (hg38) g.109466507G>A
Published as -
ISCN -
DB-ID ZBTB24_000025
Variant remarks Ty1_ZBTB24 variant construct expressed in mESCs could not restore luciferase activity of target promoter, ChIP-qPCR showed impaired binding to target promoter; experiments suggest variant is likely to be pathogenic
Reference Daxinger, in preparation 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Lucia Daxinger
Database submission license No license selected
Created by Lucia Daxinger
Date created 2019-01-29 11:22:51 +01:00 (CET)
Date last edited 2020-06-19 19:45:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB24 NM_014797.2 +/. - c.1438C>T r.(?) p.His480Tyr


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